List of variants in gene ATP6V0A2 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_012463.4(ATP6V0A2):c.*998T>C	rs12298446	0.00401
NM_012463.4(ATP6V0A2):c.*785T>C	rs146660715	0.00262
NM_012463.4(ATP6V0A2):c.1258G>T (p.Val420Leu)	rs138716143	0.00258
NM_012463.4(ATP6V0A2):c.1486G>A (p.Ala496Thr)	rs143142641	0.00035
NM_012463.4(ATP6V0A2):c.1698A>G (p.Gly566=)	rs2271659	0.00008
NM_012463.4(ATP6V0A2):c.*2485C>T	rs144043973	0.00006
NM_012463.4(ATP6V0A2):c.*2085C>G	rs185883563	0.00001
NM_012463.4(ATP6V0A2):c.2294-4G>A	rs551697992	0.00001
NM_012463.4(ATP6V0A2):c.2128_2129del	rs150303181
NM_012463.4(ATP6V0A2):c.1724+20del	rs375845531

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